Atlas FDA

DATA-ZYME UREA NITROGEN, COLORIMETRIC

FDA 510(k) clearance K801727 · decided 1980-09-09

Clearance details

K-number
K801727
Device name
DATA-ZYME UREA NITROGEN, COLORIMETRIC
Applicant
Data Medical Associates, Inc.
Decision
Substantially Equivalent
Date received
1980-07-24
Decision date
1980-09-09
Days to decision
47 days
Clearance type
Traditional
Product code
CDL
Device class
2
Regulation number
862.1770
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RAICHEM(TM) UREA NITROGEN (COLOR) REAGENT (K896845)Reagents Applications, Inc.1990-02-16
STANBIO ENZYMATIC UREA NITROGEN DETERMINAT #2010 (K893128)Stanbio Laboratory1989-07-25
COLORIMETRIC BUN REAGENT KIT (K871651)Biochemical Trade, Inc.1987-05-12
UREA NITROGEN(BUN), COLORIMETRIC METHOD (K864742)Tech-Co, Inc.1987-01-13
UREA NITROGEN TEST (K863889)U. S. Diagnostics, Inc.1986-11-24
UREAFAST (K863076)J. D. Assoc.1986-09-09
BUN (ENZYMATIC BERTHELOT) REAGENT SET (K860154)Sterling Diagnostics, Inc.1986-02-06
COLORIMETRIC BUN (K831414)Bio-Analytics Laboratories, Inc.1983-06-16
UREA NITROGEN REAGENT SET (MOD. BERTHEL (K822237)Sterling Biochemical, Inc.1982-08-16
EUROCHIMA UREA NITROGEN (K810261)Volu Sol Medical Industries1981-02-10
BUN-COLOR 2, BLOOD UREA NITROGEN TEST (K800902)Sclavo, Inc.1980-06-09
ELVI BLOOD UREA NITROGEN (K792417)Volu Sol Medical Industries1979-12-07

Recalls involving this device

No recalls on record reference this clearance.